Canonical Allele Identifier: CA1573933720
Gene:

Linked Data

dbSNP Id: rs1780063684

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661082A>T , CM000667.2:g.113661082A>T GRCh38
NC_000005.9:g.112996779A>T , CM000667.1:g.112996779A>T GRCh37
NC_000005.8:g.113024678A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27718A>T